The following data is part of a premarket notification filed by Steri-oss, Inc. with the FDA for Tomograph Accessories.
Device ID | K962120 |
510k Number | K962120 |
Device Name: | TOMOGRAPH ACCESSORIES |
Classification | Unit, X-ray, Extraoral With Timer |
Applicant | STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
Contact | Paul Gasser |
Correspondent | Paul Gasser STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
Product Code | EHD |
CFR Regulation Number | 872.1800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-31 |
Decision Date | 1996-07-25 |
Summary: | summary |